Roy Amrita Arup, Pandey Abhijeet, Dhas Namdev, Hegde Manasa Manjunath, Parekh Harendra S, Andugulapati Sai Balaji, Nandakumar Krishnadas, Satish Rao Bola Sadashiva, Mutalik Srinivas
Department of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal 576104, Karnataka, India.
Global Drug Development/Technical Research and Development, Novartis Healthcare Pvt. Ltd., Genome Valley, Hyderabad 500081, Telangana, India.
Adv Pharmacol Pharm Sci. 2025 Apr 24;2025:1847197. doi: 10.1155/adpp/1847197. eCollection 2025.
Heat-shock protein 70 (HSP70) and nanotechnology have emerged as promising avenues in glioblastoma multiforme (GBM) therapy, addressing the critical challenges posed by its aggressive nature and therapeutic resistance. HSP70's dual role in cellular stress response and tumour survival emphasises its potential as both a biomarker and therapeutic target. This review explores the innovative integration of HSP70 with nanotechnology, emphasising advancements in imaging, drug delivery and combination therapies. Nanoparticles, including SPIONs, liposomes, gold nanoparticles and metal-organic frameworks, demonstrate enhanced targeting and therapeutic efficacy through HSP70 modulation. Functionalized nanocarriers exploit HSP70's tumour-specific overexpression to improve drug delivery, minimise off-target effects and overcome the blood-brain barrier. Emerging strategies such as chemophototherapy, immunotherapy and photothermal therapy leverage HSP70's interactions within the tumour microenvironment, enabling synergistic treatment modalities. The review also highlights translational challenges, including heterogeneity of GBM, regulatory hurdles and variability in the enhanced permeability and retention (EPR) effect. Integrating computational modelling, personalised approaches and adaptive trial designs is crucial for clinical translation. By bridging nanotechnology and molecular biology, HSP70-targeted strategies hold transformative potential to redefine GBM diagnosis and treatment, offering hope for improved survival and quality of life. ClinicalTrials.gov identifier: NCT00054041 and NCT04628806.
热休克蛋白70(HSP70)和纳米技术已成为多形性胶质母细胞瘤(GBM)治疗中很有前景的途径,可应对其侵袭性本质和治疗抗性带来的严峻挑战。HSP70在细胞应激反应和肿瘤存活中的双重作用凸显了其作为生物标志物和治疗靶点的潜力。本综述探讨了HSP70与纳米技术的创新性整合,重点介绍了成像、药物递送和联合治疗方面的进展。包括超顺磁性氧化铁纳米颗粒(SPIONs)、脂质体、金纳米颗粒和金属有机框架在内的纳米颗粒,通过HSP70调节显示出增强的靶向性和治疗效果。功能化纳米载体利用HSP70在肿瘤中的特异性过表达来改善药物递送、最小化脱靶效应并克服血脑屏障。化学光疗、免疫疗法和光热疗法等新兴策略利用HSP70在肿瘤微环境中的相互作用,实现协同治疗模式。该综述还强调了转化方面的挑战,包括GBM的异质性、监管障碍以及增强的通透性和滞留(EPR)效应的可变性。整合计算模型、个性化方法和适应性试验设计对于临床转化至关重要。通过将纳米技术与分子生物学相结合,以HSP70为靶点的策略具有重新定义GBM诊断和治疗的变革潜力,为提高生存率和生活质量带来希望。 临床试验注册号:NCT00054041和NCT04628806。